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Molecular characterization of Theileria parasites: application to the epidemiology of theileriosis in Zimbabwe

Published online by Cambridge University Press:  06 April 2009

R. P. Bishop
Affiliation:
International Laboratory for Research on Animal Diseases (ILRAD), P.O. Box 30709 Nairobi, Kenya
P.R. Spooner
Affiliation:
International Laboratory for Research on Animal Diseases (ILRAD), P.O. Box 30709 Nairobi, Kenya
G. K. Kanhai
Affiliation:
FAO Project, GCP/ZIM/013/DEN, P.O. Box 3730, Harare, Zimbabwe
J. Kiarie
Affiliation:
International Laboratory for Research on Animal Diseases (ILRAD), P.O. Box 30709 Nairobi, Kenya
A. A. Latif
Affiliation:
FAO Project, GCP/ZIM/013/DEN, P.O. Box 3730, Harare, Zimbabwe
T. Hove
Affiliation:
Veterinary Research Laboratory, P.O. Box 8101, Causeway, Harare, Zimbabwe
S. Masaka
Affiliation:
Veterinary Research Laboratory, P.O. Box 8101, Causeway, Harare, Zimbabwe
T. T. Dolan
Affiliation:
International Laboratory for Research on Animal Diseases (ILRAD), P.O. Box 30709 Nairobi, Kenya

Extract

Forty Theileria schizont-infected lymphocyte culture isolates from Zimbabwe were characterized using a panel of antischizont monoclonal antibodies (MAbs) and 4 Theileria parva DNA probes containing cloned extrachromosomal element, Tpr repetitive, ribosomal and telomeric sequences. The Theileria isolates were assigned as T. parva or T. taurotragi on the basis of reactivities with MAbs and restriction fragment length polymorphisms (RFLPs) detected using the extra chromosomal element probe. Cattle-derived T. parva isolates were relatively homogeneous on the basis of reactivities with MAbs and RFLPs detected using Tpr repetitive and ribosomal DNA probes. In contrast to previous results from Kenya, most of the cattle-derived isolates from Zimbabwe exhibited very similar Tpr restriction fragment patterns, although the Tpr genotypes of buffalo-derived isolates were heterogeneous. This suggests that selection for a particular Tpr genotype may be occurring in cattle. Many isolates with similar Tpr genotypes were differentiated by RFLPs detected using the telomeric DNA probe. The T. parva Boleni immunizing stock was distinguished from all other isolates by telomeric RFLPs. The T. parva Boleni Tpr repetitive DNA probe cross-hybridized with T. taurotragi DNA and detected RFLPs between different T. taurotragi isolates.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1994

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References

REFERENCES

Allsopp, B. A. & Allsopp, M. T. E. P. (1988). Theileria parva: genomic DNA studies reveal intra-specific sequence diversity. Molecular and Biochemical Parasitology 28, 7784.CrossRefGoogle ScholarPubMed
Bailey, K. P. (1960). Notes on the rearing of Rhipicephalus appendiculatus and their infection with Theileria parva for experimental transmission. Bulletin of Epizootic Diseases of Africa 8, 3343.Google Scholar
Baylis, H. A., Sohal, S. K., Carrington, M., Bishop, R. P. & Allsopp, B. A. (1991). An unusual repetitive gene family in Theileria parva which is stage specifically transcribed. Molecular and Biochemical Parasitology 49, 133–42.CrossRefGoogle ScholarPubMed
Bishop, R. P., Sohanpal, B., Kariuki, D. P., Young, A. S., Nene, V., Baylis, H., Allsopp, B. A., Spooner, P. R., Dolan, T. T. & Morzaria, S. P. (1992). Detection of a carrier state in Theileria parva-infected cattle by the polymerase chain reaction. Parasitology 104, 215–32.CrossRefGoogle ScholarPubMed
Bishop, R. P., Sohanpal, B. K., Allsopp, B. A., Spooner, P. R., Dolan, T. T. & Morzaria, S. P. (1993). Detection of polymorphisms among Theileria parva stocks using repetitive, telomeric and ribosomal DNA probes and anti-schizont monoclonal antibodies. Parasitology 107, 1931.CrossRefGoogle ScholarPubMed
Brocklesby, D. W., Barnett, S. F. & Scott, G. R. (1961). Morbidity and mortality rates in East Coast fever (Theileria parva infection) and their application to drug screening procedures. British Veterinary Journal 17, 529–31.CrossRefGoogle Scholar
Brown, C. G. D. (1979). Propagation of Theileria. In Practical Tissue Culture Applications, (ed. Maramorosch, K. & Hirumi, H.), pp. 223–45. NewYork: Academic Press.Google Scholar
Conrad, P. A., Iams, K., Brown, W. C., Sohanpal, B. & Ole-Moiyoi, O. (1987). DNA probes detect genomic diversity in Theileria parva stocks. Molecular and Biochemical Parasitology 25, 213–26.CrossRefGoogle ScholarPubMed
Conrad, P. A., Ole-Moiyoi, O. K., Baldwin, C. L., Dolan, T. T., O'Callaghan, C. J., Njamunggeh, R. E. G., Grootenhuis, J. G., Stagg, D. A., Leitch, B. L. & Young, A. S. (1989). Characterization of buffalo- derived theilerial parasites with monoclonal antibodies and DNA probes. Parasitology 98, 179–88.CrossRefGoogle ScholarPubMed
Cunningham, M. P., Brown, C. G. D., Burridge, M. J. & Purnell, R. E. (1973). Cryopreservation of infective particles of Theileria parva. International Journal for Parasitology 3, 583–7.CrossRefGoogle ScholarPubMed
Dolan, T. T. (1987). Immunization to control East Coast fever. Parasitology Today 3, 410.Google ScholarPubMed
Grootenhuis, J. G., Young, A. S., Dolan, T. T. & Stagg, D. A. (1979). Characteristics of Theileria species (eland) infections in eland and cattle. Research in Veterinary Science 27, 5968.CrossRefGoogle ScholarPubMed
Hove, T., Musisi, F. L., Kanhai, G. K., Latif, A., Masaka, S., Munatswa, F. C., Pegram, R. G., Kamwendo, S. P., Quiroga, J. C., Mwangondwe, R. & Dolan, T. T. (1994). Challenge of Theileria parva (Boleni)immunized cattle with selected East African Theileria stocks. Tropical Animal Health and Production (in the Press).Google Scholar
Irvin, A. D., Dobbelaere, D. A. E., Mwamachi, D. M., Minami, M., Spooner, P. R. & Ocama, J. G. R. (1983). Immunisation against East Coast fever: Correlation between monoclonal antibody profiles of Theileria parva stocks and cross immunity in vivo. Research in Veterinary Science 35, 341–6.CrossRefGoogle ScholarPubMed
Kairo, H., Fairlamb, A. H., Gobright, E. & Nene, V. (1994). A linear 7·1 kb DNA molecule of Theileria parva has scrambled rDNA sequences and open reading frames for mitochondrially encoded proteins. EMBO Journal (in the Press).CrossRefGoogle ScholarPubMed
Kearney, J. F., Radbruch, A., Liesegang, B. & Rajewsky, K. (1979). A new mouse myeloma cell line that has lost immunoglobulin expression but permits construction of antibody secreting hybrid cell lines. Journal of Immunology 123, 1548–50.CrossRefGoogle ScholarPubMed
Kibe, M. K., Ole-Moi Yoi, O. K., Nene, V., Khan, B., Allsopp, B. A., Collins, N. E., Morzaria, S. P., Gobright, E. I. & Bishop, R. P. (1994). Organization of Theileria parva ribosomal RNA genes: evidence for two single copy units. Molecular and Biochemical Parasitology (in the Press).CrossRefGoogle ScholarPubMed
Koch, H. T., Ocama, J. G. R., Munatswa, F. C., Byrom, B., Norval, R. A. I., Spooner, P. R., Conrad, P. A. & Irvin, A. D. (1988). Isolation and characterization of bovine Theileria parasites in Zimbabwe. Veterinary Parasitology 28, 1932.CrossRefGoogle ScholarPubMed
Koch, H. T., Kambeva, L., Ocama, J. G. R., Munatswa, F. C., Franssen, F. F. J., Uilenberg, G., Dolan, T. T. & Norval, R. A. I. (1990 a). Immunization of cattle against Theileria parva bovis and their exposure to natural challenge. Veterinary Parasitology 37, 185–96.CrossRefGoogle ScholarPubMed
Koch, H. T., Kambeva, L., Norval, R. A. I., Ocama, J. G. R., Masaka, S., Munatswa, F. C., Honhold, N. & Irvin, A. D. (1990 b). Age resistance to Theileria parva bovis infection in calves. Veterinary Parasitology 37, 197206.CrossRefGoogle ScholarPubMed
Lawrence, J. A. (1977). The serological relationship between Theileria parva (Muguga) and Theileria lawrencei from Rhodesia. Veterinary Record 100, 470–2.CrossRefGoogle ScholarPubMed
Lawrence, J. A. (1979). The differential diagnosis of the bovine theilerias of Southern Africa. Journal of the South African Veterinary Association 50, 311–13.Google ScholarPubMed
Lawrence, J. A. & Mackenzie, P. K. I. (1980). Isolation of a non-pathogenic Theileria of cattle transmitted by Rhipicephalus appendiculatus. Zimbabwe Veterinary Journal 11, 2735.Google Scholar
Lawrence, J. A. & Norval, R. A. I. (1979). A history of ticks and tick-borne diseases of cattle in Rhodesia. Rhodesian Veterinary Journal 10, 2840.Google Scholar
Matson, B. A. (1967). Theileriosis in Rhodesia: I. A study of diagnostic specimens over two seasons. Journal of the South African Veterinary Medical Association 38, 93102.Google Scholar
Melhorn, H. & Schein, E. (1984). The piroplasms: life cycle and sexual stages. Advances in Parasitology 23, 37103.CrossRefGoogle Scholar
Minami, T., Spooner, P. R., Irvin, A. D., Ocama, J. G. R., Dobbelaere, D. A. E. & Fujinaga, T. (1983). Characterisation of stocks of Theileria parva by monoclonal antibody profiles. Research in Veterinary Science 35, 334–40.CrossRefGoogle ScholarPubMed
Morzaria, S. P., Spooner, S. P., Bishop, R. P., Musoke, A. J. & Young, J. R. (1990). SfiI and NotI polymorphisms in Theileria stocks detected by pulsed field gel electrophoresis. Molecular and Biochemical Parasitology 40, 203–12.CrossRefGoogle ScholarPubMed
Morzaria, S. P., Young, J. R., Spooner, P. R., Dolan, T. T., Young, A. S. & Bishop, R. P. (1992). Evidence of a sexual cycle in Theileria parva and characterisation of the recombinants. In First Internaional Conference on Tick-Borne Pathogens at the Host–Vector Interface–An Agenda for Research: Proceedings and Abstracts, (ed. Munderloch, U. G. & Kurtti, T. J.), pp. 7174. Saint Paul, Minnesota: University of Minnesota College of Agriculture.Google Scholar
Nene, V., Shaw, M., Morzaria, S. & Fairlamb, A. (1991). A linear 7·1 kb DNA molecule encodes a subset of Theileria parva mitochondrial proteins. Annual Scientific Report, pp. 15. ILRAD. Nairobi. Kenya.Google Scholar
Pearson, T. W., Pinder, M., Roelants, G. E., Kar, S. K., Lundin, L. B., Mayor-Withey, K. S. & Hewett, R. S. (1980). Methods for derivation and detection of anti- parasite monoclonal antibodies. Journal of Immunological Methods 34, 141–54.CrossRefGoogle ScholarPubMed
Pegram, R. G., James, A. D., Bamhara, C., Dolan, T. T., Hove, T., Kanhai, G. K. & Latif, A. A. (1994). Effects of immunization against Theileria parva on beef cattle productivity and economics of control options. Tropical Animal Health and Production (in the Press).Google Scholar
Ponzi, M., Pace, T., Dore, E. & Frontali, C. (1985). Identification of a telomeric DNA sequence in Plasmodium berghei. EMBO Journal 4, 2991–5.CrossRefGoogle ScholarPubMed
Radley, D. E., Brown, C. G. D., Burridge, M. J., Cunningham, M. P., Kirimi, I. M., Purnell, R. E. & Young, A. S. (1975). East Coast fever, 1. Chemoprophylactic immunization of cattle against Theileria parva (Muguga) and five theilerial strains. Veterinary Parasitology 1, 3541.CrossRefGoogle Scholar
Sambrook, J., Fritsch, E. F. & Maniatis, T. (1989). Molecular Cloning: a Laboratory Manual, 2nd Edn.Cold Spring Harbour, New York: Cold Spring Harbour Laboratory.Google Scholar
Stagg, D. A., Young, A. S., Leitch, B. L., Grootenhuis, J. G. & Dolan, T. T. (1983). Infection of mammalian cells with Theileria species. Parasitology 86, 243–54.CrossRefGoogle ScholarPubMed
Uilenberg, G. (1981). Theilerial species of domestic livestock. In Advances in the Control of Theileriosis (ed. Irvin, A. D., Cunningham, M. P. & Young, A. S.), pp. 437. The Hague: Martinhus Nijhoff.CrossRefGoogle Scholar
Uilenberg, G., Perie, N. M., Lawrence, J. A., De Vos, A. J., Paling, R. W. & Spanjer, A. A. M. (1982). Causal agents of bovine theileriasis in Southern Africa. Tropical Animal Health and Production 14, 127–40.CrossRefGoogle ScholarPubMed
Young, R. A., Mehra, V., Sweetser, D., Buchanan, T., Clark-Curtis, J., Davis, R. W. & Bloom, B. R. (1985). Genes for the major protein antigens of the leprosy parasite Mycobacterium leprae. Nature, London 316, 450–2.CrossRefGoogle ScholarPubMed